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Intranasal oxytocin for treating mother-infant attachment problems in postnatal depression

Crossover trial of intranasal oxytocin for treating mother-infant attachment problems in postnatal depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN92184014
Enrollment
10
Registered
2012-03-08
Start date
2011-12-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postnatal mental health / mother-infant attachment Pregnancy and Childbirth Postnatal depression

Interventions

Intranasal administration of 24IU Syntocinon® (oxytocin) versus Intranasal administration of placebo (0.9% sodium chloride solution) Video will be recorded of the mother-infant interaction following

Sponsors

NHS Greater Glasgow & Clyde (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Mother with history of low mood (recorded Edinburgh Postnatal Depression Score of ten or greater) with baby aged 8-16 weeks 2. Mother aged 18 ? 50 years

Exclusion criteria

Exclusion criteria: 1. Baby born before 38 weeks 2. Significant obstetric complications 3. Significant medical condition of mother or baby 4. Substantial neurological or visual impairment of mother or baby 5. Mother non-English speaking 6. Mother continuing to breast feed 7. Mother has physical condition which might affect nasal drug absorption (eg. URTI) 8. Mother responsible for care of another child at time of home visit 9. Mother pregnant 10. Mothers on antidepressant medication will not be excluded from the study; however we will record if a subject is on medication

Design outcomes

Primary

MeasureTime frame
Duration of mutual eye region gaze between mother and baby

Secondary

MeasureTime frame
1. CARE index will be calculated from the video footage (ie. at 45mins post-spray administration on both occasions) 2. Neonatal perception index will be completed at 0 and 45 minutes each time

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026